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Piroxicam attenuates 3-nitropropionic acid-induced brain oxidative stress and behavioral alteration in mice

机译:吡罗昔康减轻小鼠3-硝基丙酸诱导的脑氧化应激和行为改变

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摘要

3-Nitropropionic acid (3-NP) is a fungal toxin that produces Huntington's disease like symptoms in both animals and humans. Piroxicam, a non-selective cyclooxygenase (COX) inhibitor, used as anti-inflammatory agent and also known to decrease free oxygen radical production. In this study, the effect of piroxicam was evaluated against 3-NP-induced brain oxidative stress and behavioral alteration in mice. Adult male Swiss albino mice were injected with vehicle/piroxicam (10 and 20 mg/kg, i.p.) 30 min before 3-NP challenge (15 mg/kg, i.p.) regularly for 14 days. Body weights of the mice were measured on alternative days of the experiment. At the end of the treatment schedule, mice were evaluated for behavioral alterations (movement analysis, locomotor test, beam walking test and hanging wire test) and brain homogenates were used for the estimation of oxidative stress markers (lipid peroxidation, reduced glutathione and catalase). Administration of 3-NP significantly altered the behavioral activities and brain antioxidant status in mice. Piroxicam, at both the tested doses, caused a significant reversal of 3-NP-induced behavioral alterations and oxidative stress in mice. These findings suggest piroxicam protects the mice against 3-NP-induced brain oxidative stress and behavioral alteration. The antioxidant properties of piroxicam may be responsible for the observed beneficial actions.
机译:3-硝基丙酸(3-NP)是一种真菌毒素,会在动物和人类中产生类似亨廷顿氏病的症状。吡罗昔康(Piroxicam)是一种非选择性的环氧合酶(COX)抑制剂,用作抗炎药,也已知会减少自由基产生。在这项研究中,评估了吡罗昔康对3-NP诱导的小鼠脑部氧化应激和行为改变的影响。成年雄性瑞士白化病小鼠在接受3-NP攻击(15 mg / kg,腹膜内)前30分钟定期注射媒介物/吡罗昔康(10和20 mg / kg,腹膜内)14天。在实验的另外几天测量小鼠的体重。在治疗计划结束时,评估小鼠的行为改变(运动分析,运动测试,束步测试和吊线测试),并使用脑匀浆评估氧化应激指标(脂质过氧化,还原型谷胱甘肽和过氧化氢酶) 。 3-NP的使用显着改变了小鼠的行为活动和脑部抗氧化状态。两种测试剂量的吡罗昔康均可导致小鼠3-NP诱导的行为改变和氧化应激的显着逆转。这些发现表明吡罗昔康可以保护小鼠免受3-NP诱导的脑氧化应激和行为改变的影响。吡罗昔康的抗氧化特性可能是所观察到的有益作用的原因。

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